Literature DB >> 22258366

Impact of a cancer clinical trials web site on discussions about trial participation: a cluster randomized trial.

R F Dear1, A L Barratt, L M Askie, P N Butow, K McGeechan, S Crossing, D C Currow, M H N Tattersall.   

Abstract

BACKGROUND: Cancer patients want access to reliable information about currently recruiting clinical trials. PATIENTS AND METHODS: Oncologists and their patients were randomly assigned to access a consumer-friendly cancer clinical trials web site [Australian Cancer Trials (ACT), www.australiancancertrials.gov.au] or to usual care in a cluster randomized controlled trial. The primary outcome, measured from audio recordings of oncologist-patient consultations, was the proportion of patients with whom participation in any clinical trial was discussed. Analysis was by intention-to-treat accounting for clustering and stratification.
RESULTS: Thirty medical oncologists and 493 patients were recruited. Overall, 46% of consultations in the intervention group compared with 34% in the control group contained a discussion about clinical trials (P=0.08). The mean consultation length in both groups was 29 min (P=0.69). The proportion consenting to a trial was 10% in both groups (P=0.65). Patients' knowledge about randomized trials was lower in the intervention than the control group (mean score 3.0 versus 3.3, P=0.03) but decisional conflict scores were similar (mean score 42 versus 43, P=0.83).
CONCLUSIONS: Good communication between patients and physicians is essential. Within this context, a web site such as Australian Cancer Trials may be an important tool to encourage discussion about clinical trial participation.

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Mesh:

Year:  2012        PMID: 22258366     DOI: 10.1093/annonc/mdr585

Source DB:  PubMed          Journal:  Ann Oncol        ISSN: 0923-7534            Impact factor:   32.976


  9 in total

1.  Culturally and linguistically diverse patient participation in glioma research.

Authors:  Zarnie Lwin; Alexander Broom; Rasha Cosman; Ann Livingstone; Kate Sawkins; Phillip Good; Emma Kirby; Eng-Siew Koh; Elizabeth Hovey
Journal:  Neurooncol Pract       Date:  2014-06-25

Review 2.  Strategies to improve recruitment to randomised trials.

Authors:  Shaun Treweek; Marie Pitkethly; Jonathan Cook; Cynthia Fraser; Elizabeth Mitchell; Frank Sullivan; Catherine Jackson; Tyna K Taskila; Heidi Gardner
Journal:  Cochrane Database Syst Rev       Date:  2018-02-22

3.  A European multi-language initiative to make the general population aware of independent clinical research: the European Communication on Research Awareness Need project.

Authors:  Paola Mosconi; Gerd Antes; Giorgio Barbareschi; Amanda Burls; Jacques Demotes-Mainard; Iain Chalmers; Cinzia Colombo; Silvio Garattini; Christian Gluud; Gill Gyte; Catherine Mcllwain; Matt Penfold; Nils Post; Roberto Satolli; Maria Rosa Valetto; Brian West; Stephanie Wolff
Journal:  Trials       Date:  2016-01-12       Impact factor: 2.279

4.  Patients' reasoning regarding the decision to participate in clinical cancer trials: an interview study.

Authors:  Pia Dellson; Kerstin Nilsson; Helena Jernström; Christina Carlsson
Journal:  Trials       Date:  2018-09-29       Impact factor: 2.279

5.  A step towards equitable clinical trial recruitment: a protocol for the development and preliminary testing of an online prostate cancer health information and clinical trial matching tool.

Authors:  Hala T Borno; Brian M Bakke; Celia Kaplan; Anke Hebig-Prophet; Jessica Chao; Yoon-Ji Kim; Jan Yeager; Pelin Cinar; Eric Small; Christy Boscardin; Ralph Gonzales
Journal:  Pilot Feasibility Stud       Date:  2019-11-07

Review 6.  Decision aids for people considering taking part in clinical trials.

Authors:  Katie Gillies; Seonaidh C Cotton; Jamie C Brehaut; Mary C Politi; Zoe Skea
Journal:  Cochrane Database Syst Rev       Date:  2015-11-27

7.  Interdisciplinary decision making in prostate cancer therapy - 5-years' time trends at the Interdisciplinary Prostate Cancer Center (IPC) of the Charité Berlin.

Authors:  Daniel Baumunk; Roman Reunkoff; Julien Kushner; Alexandra Baumunk; Carsten Kempkensteffen; Ursula Steiner; Steffen Weikert; Lutz Moser; Mark Schrader; Stefan Höcht; Thomas Wiegel; Kurt Miller; Martin Schostak
Journal:  BMC Med Inform Decis Mak       Date:  2013-08-05       Impact factor: 2.796

8.  Patient representatives' views on patient information in clinical cancer trials.

Authors:  Pia Dellson; Mef Nilbert; Christina Carlsson
Journal:  BMC Health Serv Res       Date:  2016-02-01       Impact factor: 2.655

9.  Impact of patient and public involvement on enrolment and retention in clinical trials: systematic review and meta-analysis.

Authors:  Joanna C Crocker; Ignacio Ricci-Cabello; Adwoa Parker; Jennifer A Hirst; Alan Chant; Sophie Petit-Zeman; David Evans; Sian Rees
Journal:  BMJ       Date:  2018-11-28
  9 in total

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